(R)-(-)-1-Cyclohexylethylamine, ChiPros 98%, ee 94+%
(R)-(-)-1-Cyclohexylethylamine, ChiPros 98%, ee 94+%
(R)-(-)-1-Cyclohexylethylamine, ChiPros 98%, ee 94+%
(R)-(-)-1-Cyclohexylethylamine, ChiPros 98%, ee 94+%
Thermo Scientific Chemicals

(R)-(-)-1-Cyclohexylethylamine, ChiPros 98%, ee 94+%

CAS: 5913-13-3 | C8H17N | 127.23 g/mol
Quantity:
1 g
5 g
Catalog number L19051.06
also known as L19051-06
Price (JPY)
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5 g
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Chemical Identifiers
CAS5913-13-3
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥97.5%
Optical Rotation-4° ±0.5° (neat)
Refractive Index1.4600-1.4640 @ 20°C
(R)-(-)-1-Cyclohexylethylamine is used in the preparation of benzylidene(1-cyclohexylethyl)amine by reacting with benzaldehyde. It is also used to prepare chiral polymethacrylamides, which are employed as stationary phases for the liquid-chromatographic resolution of racemic amides. In addition to this, it is used in the preparation of polyamides bound to silica gel for high performance liquid chromatography, which are pressure-stable.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(R)-(-)-1-Cyclohexylethylamine is used in the preparation of benzylidene(1-cyclohexylethyl)amine by reacting with benzaldehyde. It is also used to prepare chiral polymethacrylamides, which are employed as stationary phases for the liquid-chromatographic resolution of racemic amides. In addition to this, it is used in the preparation of polyamides bound to silica gel for high performance liquid chromatography, which are pressure-stable.

Solubility
Miscible with acetone, chloroform,dimethyl sulfoxide, ethanol, methanol, ether, petroleum ether and dichloromethane. Insoluble in water.

Notes
Hygroscopic. Air sensitive. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Singh, M.; Bhushan, R. A novel approach for enantioseparation as applied to (RS)-etodolac from pharmaceutical formulations: LC MS and density functional theory support for confirmation of diastereomers so separated. Biomed. Chromatogr. 2015, 29 (9), 1330-1337.
  2. Eerdun, C.; Hisanaga, S.; Setsune, J. I. One-Handed Single Helicates of Dinickel(II) Benzenehexapyrrole-alpha,μ-diimine with an Amine Chiral Source. Chem. Eur. J. 2015, 21 (1), 239-246.